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Peer-reviewed veterinary case report

Cat with seizures and bone pain diagnosed with rare vitamin D rickets

By T. Teshima et al.·Published in BMC Veterinary Research·2019·View original on Semantic Scholar

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Original publication title: A genetic variant of CYP2R1 identified in a cat with type 1B vitamin D-dependent rickets: a case report

Species:
cat
Brain & nervesCats

Plain-English summary

A 3-month-old female domestic short-haired cat was brought to the vet after experiencing seizures, lethargy, and generalized pain. Blood tests revealed low levels of calcium and vitamin D, and X-rays showed skeletal issues. Initially thought to be a simple vitamin D deficiency, further testing indicated a genetic problem affecting vitamin D metabolism. After identifying a specific genetic mutation, the vet started the cat on calcitriol, a form of vitamin D, which significantly improved her condition.

People also search for: cat seizures treatment · vitamin D deficiency in cats · kitten lethargy causes

Abstract

BackgroundVitamin D-dependent rickets is rare in animals and humans. Several types of this condition are associated with genetic variants related to vitamin D metabolism. This is the first report of type 1B vitamin D-dependent rickets in a cat.Case presentationHere, we describe the case of a 3-month-old female domestic short-haired cat previously fed on commercial kitten food that presented at our clinic with seizures, lethargy, and generalized pain. Serum and ionized calcium concentrations and 1,25-dihydroxycholecalciferol in this cat were low, and radiographs showed skeletal demineralization and abnormally wide growth plates on the long bones. Initially, simple vitamin D deficiency was suspected; however, the cat’s profile, which included fed a well-balanced commercial diet, together with the findings of additional laboratory tests and the cat’s unresponsiveness to various treatments, raised the suspicion of vitamin D-dependent rickets. Examination of the DNA sequences of CYP2R1 and CYP27B1 genes, which are genes linked with vitamin D metabolism, showed a CYP2R1 frameshift mutation in exon 5 (where T is deleted at position c.1386). This mutation alters the amino acid sequence from position 462, while the stop codon introduced at position 481 prematurely truncates the 501 amino acid full-length protein. With this knowledge, a new treatment regime based on a standard dose of calcitriol was started and this markedly improved the cat’s condition.ConclusionsTo the best of our knowledge, the present case is the first description of type 1B vitamin D-dependent rickets linked with a genetic variant of CYP2R1 in a cat.

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Original publication on Semantic Scholar: https://www.semanticscholar.org/paper/30777056